Fant 10001 publikasjoner. Viser side 48 av 401:
The oil and gas (O&G) sector is a significant source of methane (CH4) emissions. Quantifying these emissions remains challenging, with many studies highlighting discrepancies between measurements and inventory-based estimates. In this study, we present CH4 emission fluxes from 21 offshore O&G facilities collected in 10 O&G fields over two regions of the Norwegian continental shelf in 2019. Emissions of CH4 derived from measurements during 13 aircraft surveys were found to range from 2.6 to 1200 t yr−1 (with a mean of 211 t yr−1 across all 21 facilities). Comparing this with aggregated operator-reported facility emissions for 2019, we found excellent agreement (within 1σ uncertainty), with mean aircraft-measured fluxes only 16 % lower than those reported by operators. We also compared aircraft-derived fluxes with facility fluxes extracted from a global gridded fossil fuel CH4 emission inventory compiled for 2016. We found that the measured emissions were 42 % larger than the inventory for the area covered by this study, for the 21 facilities surveyed (in aggregate). We interpret this large discrepancy not to reflect a systematic error in the operator-reported emissions, which agree with measurements, but rather the representativity of the global inventory due to the methodology used to construct it and the fact that the inventory was compiled for 2016 (and thus not representative of emissions in 2019). This highlights the need for timely and up-to-date inventories for use in research and policy. The variable nature of CH4 emissions from individual facilities requires knowledge of facility operational status during measurements for data to be useful in prioritising targeted emission mitigation solutions. Future surveys of individual facilities would benefit from knowledge of facility operational status over time. Field-specific aggregated emissions (and uncertainty statistics), as presented here for the Norwegian Sea, can be meaningfully estimated from intensive aircraft surveys. However, field-specific estimates cannot be reliably extrapolated to other production fields without their own tailored surveys, which would need to capture a range of facility designs, oil and gas production volumes, and facility ages. For year-on-year comparison to annually updated inventories and regulatory emission reporting, analogous annual surveys would be needed for meaningful top-down validation. In summary, this study demonstrates the importance and accuracy of detailed, facility-level emission accounting and reporting by operators and the use of airborne measurement approaches to validate bottom-up accounting.
2022
2022
The global monitoring plan of the Minamata Convention on Mercury was established to generate long-term data necessary for evaluating the effectiveness of regulatory measures at a global scale. After 25 years of monitoring (since 1995), Mace Head is one of the atmospheric monitoring stations with the longest mercury record and has produced sufficient data for the analysis of temporal trends of total gaseous mercury (TGM) in Europe and the North Atlantic. Using concentration-weighted trajectories for atmospheric mercury measured at Mace Head as well as another five locations in Europe, Amderma, Andøya, Villum, Waldhof and Zeppelin, we identify the regional probabilistic source contribution factor and its changes for the period of 1996 to 2019. Temporal trends indicate that concentrations of mercury in the atmosphere in Europe and the North Atlantic have declined significantly over the past 25 years at a non-monotonic rate averaging 0.03 . Concentrations of TGM at remote marine sites were shown to be affected by continental long-range transport, and evaluation of reanalysis back trajectories displays a significant decrease in TGM in continental air masses from Europe in the last 2 decades. In addition, using the relationship between mercury and other atmospheric trace gases that could serve as a source signature, we perform factorization regression analysis, based on positive rotatable factorization to solve probabilistic mass functions. We reconstructed atmospheric mercury concentration and assessed the contribution of the major natural and anthropogenic sources. The results reveal that the observed downward trend in the atmospheric mercury is mainly associated with a factor with a high load of long-lived anthropogenic species.
2022
Herring gulls (Larus argentatus) are opportunistic feeders, resulting in contaminant exposure depending on area and habitat. We compared contaminant concentrations and dietary markers between two herring gull breeding colonies with different distances to extensive human activity and presumed contaminant exposure from the local marine diet. Furthermore, we investigated the integrity of DNA in white blood cells and sensitivity to oxidative stress. We analyzed blood from 15 herring gulls from each colony—the urban Oslofjord near the Norwegian capital Oslo in the temperate region and the remote Hornøya island in northern Norway, on the Barents Sea coast. Based on d13C and d34S, the dietary sources of urban gulls differed, with some individuals having a marine and others a more terrestrial dietary signal. All remote gulls had a marine dietary signal and higher relative trophic level than the urban marine feeding gulls. Concentrations (mean ± standard deviation [SD]) of most persistent organic pollutants, such as polychlorinated biphenyl ethers (PCBs) and perfluorooctane sulfonic acid (PFOS), were higher in urban marine (PCB153 17 ± 17 ng/g wet weight, PFOS 25 ± 21 ng/g wet wt) than urban terrestrial feeders (PCB153 3.7 ± 2.4 ng/g wet wt, PFOS 6.7 ± 10 ng/g wet wt). Despite feeding at a higher trophic level (d15N), the remote gulls (PCB153 17 ± 1221 ng/g wet wt, PFOS 19 ± 1421 ng/g wet wt) were similar to the urban marine feeders. Cyclic volatile methyl siloxanes were detected in only a few gulls, except for decamethylcyclopentasiloxane in the urban colony, which was found in 12 of 13 gulls. Only hexachlorobenzene was present in higher concentrations in the remote (2.6 ± 0.42 ng/g wet wt) compared with the urban colony (0.34 ± 0.33 ng/g wet wt). Baseline and induced DNA damage (doublestreak breaks) was higher in urban than in remote gulls for both terrestrial and marine feeders.
2022
Målinger av miljøgifter i luft ved Franzefoss Eide på Sotra og Husøya ved Kristiansund
NILU har gjennomført måleprogram for konsentrasjoner i luft ved Franzefoss Gjenvinning AS sine anlegg ved Eide på Sotra og ved Husøya ved Kristiansund. Ved Eide ble det tatt prøver i luft og analysert for prioriterte miljøgifter som dekloraner, fenoler, ftalater, PFAS, benzotriazoler, organiske tinnforbindelser, samt VOC inkludert D6, ammoniakk (NH3), gassfase HCl og hydrogensulfid (H2S). For de prioriterte miljøgiftene var de fleste prøvene under deteksjonsgrensen. De høyeste verdiene ble observert ved Lokasjon 11 Vannrenseanlegget. Ved Husøya ble det tatt prøver i luft og analysert for VOC inkludert D6, ammoniakk (NH3) og gassfase HCl. Verdiene ved Husøya var lavere enn ved Eide.
NILU
2022
2022
2022
The assessment of long-range transport potential (LRTP) is enshrined in several frameworks for chemical regulation such as the Stockholm Convention. Screening for LRTP is commonly done with the OECD Pov and LRTP Screening Tool employing two metrics, characteristic travel distance (CTD) and transfer efficiency (TE). Here we introduce a set of three alternative metrics and implement them in the Tool’s model. Each metric is expressed as a fraction of the emissions in a source region. The three metrics quantify the extent to which the chemical (i) reaches a remote region (dispersion, ϕ1), (ii) is transferred to surface media in the remote region (transfer, ϕ2), and (iii) accumulates in these surface media (accumulation, ϕ3). In contrast to CTD and TE, the emissions fractions metrics can integrate transport via water and air, enabling comprehensive LRTP assessment. Furthermore, since there is a coherent relationship between the three metrics, the new approach provides quantitative mechanistic insight into different phenomena determining LRTP. Finally, the accumulation metric, ϕ3, allows assessment of LRTP in the context of the Stockholm Convention, where the ability of a chemical to elicit adverse effects in surface media is decisive. We conclude that the emission fractions approach has the potential to reduce the risk of false positives/negatives in LRTP assessments.
2022
The greenhouse gases (GHG) emissions in the European Union (EU) are mainly caused by human activity from five sectors—power, industry, transport, buildings, and agriculture. To tackle all these challenges, the EU actions and policies have been encouraging initiatives focusing on a holistic approach but these initiatives are not enough coordinated and connected to reach the much needed impact. To strengthen the important role of regions in climate actions, and stimulate wide stakeholders’ engagement including citizens, a conceptual framework for enabling rapid and far-reaching climate actions through multi-sectoral regional adaptation pathways is hereby developed. The target audience for this framework is composed by regional policy makers, developers and fellow scientists. The scale of the framework emphasizes the regional function as an important meeting point and delivery arena for European and national climate strategies and objectives both at urban and rural level. The framework is based on transformative and no-regret measures, prioritizing the Key Community Systems (KCS) that most urgently need to be protected from climate impacts and risks.
2022
Screening of Chlorinated Paraffins, Dechloranes and UV-filters in Nordic Countries
In 2019, the Nordic screening group decided to perform a Nordic screening on chlorinated paraffins, dechloranes and UV-filters. These compounds are used in a wide range of applications. They all have long range transport characteristics and can potentially be regulated under the Stockholm POP convention. However, there are still huge data gaps, which need to be addressed in order to fulfill regulation requests. Several topics and questions were in focus for more measurements and a deeper understanding: (1) importance of long-range atmospheric transport and deposition, (2) differences/similarities in terrestrial versus marine food chains, and (3) variations between the Nordic countries and between urban and remote areas. Based on these priorities, availability of samples, and other practical reasons, samples from different Nordic countries, different environments, and both urban and remote places were selected. This study includes analysis of the compounds in air, marine and freshwater fish and marine mammals and bird eggs, but as the chlorinated paraffins also have been found to accumulate in the terrestrial food web, terrestrial mammals and bird eggs were included as well. Additionally, samples of pine needles were analysed both to look at the possibility for long range transport and to investigate it as a possible source of chlorinated paraffins for the terrestrial mammals.
Nordic Council of Ministers
2022
Mercury isotope evidence for Arctic summertime re-emission of mercury from the cryosphere
During Arctic springtime, halogen radicals oxidize atmospheric elemental mercury (Hg0), which deposits to the cryosphere. This is followed by a summertime atmospheric Hg0 peak that is thought to result mostly from terrestrial Hg inputs to the Arctic Ocean, followed by photoreduction and emission to air. The large terrestrial Hg contribution to the Arctic Ocean and global atmosphere has raised concern over the potential release of permafrost Hg, via rivers and coastal erosion, with Arctic warming. Here we investigate Hg isotope variability of Arctic atmospheric, marine, and terrestrial Hg. We observe highly characteristic Hg isotope signatures during the summertime peak that reflect re-emission of Hg deposited to the cryosphere during spring. Air mass back trajectories support a cryospheric Hg emission source but no major terrestrial source. This implies that terrestrial Hg inputs to the Arctic Ocean remain in the marine ecosystem, without substantial loss to the global atmosphere, but with possible effects on food webs.
2022
Environmental Contaminants in an Urban Fjord, 2021
This report presents data from the first year of a new 5-year period of the Urban Fjord programme. The programme started in 2013 and has since been altered/advanced. In 2021 the programme covers sampling and analyses of stormwater, river water, effluent from a wastewater treatment plant (inputs to the fjord), fjord sediment, blue mussel, cod and (river) trout, all from the Inner Oslofjord area. A total of 260 single compounds/isomers were analysed and frequent detection was found of benzothiazoles in abiotic aqueous phases, UV-compounds in most matrices, metals in all matrices, PBDEs in biota, chlorinated paraffins in all matrices and PCBs in biota and abiotic particle phases. Four
Norsk institutt for vannforskning (NIVA)
2022
2022
The historical (1835–2020) deposition of major air pollutants (SO2, NOx, O3 and PM2.5) indoors, as represented by the monumental Edvard Munch paintings (c. 220 m2) installed in 1916 in the Oslo University Aula in Norway, were approximated from the outdoor air concentrations, indoor to outdoor concentration ratios and dry deposition velocities. The annual deposition of the pollutants to the paintings was found to have been 4–25 times lower than has been reported to buildings outdoors in the urban background in the centre of Oslo. It reflected the outdoor deposition but varied less, from 0.3 to 1.2 g m−2 a−1. The accumulated deposition since 1916, and then not considering the regularly performed cleaning of the paintings, was found to have been 43 ± 13 g m−2, and 110 ± 40 g m−2 in a similar situation since 1835. The ozone deposition, and the PM2.5 deposition before the 1960s, were a relatively larger part of the accumulated total indoor (to the paintings) than reported outdoor deposition. About 18 and 33 times more O3 than NOx and PM2.5 deposition was estimated to the paintings in 2020, as compared to the about similar reported outdoor dry deposition of O3 and NOx. The deposition of PM2.5 to the paintings was probably reduced with about 62% (50–80%) after installation of mechanical filtration in 1975 and was estimated to be 0.011 (± 0.006) g m−2 in 2020.
2022
Health Risk Assessment of Air Pollution and the Impact of the New WHO Guidelines
Air pollution is a major cause of premature death and disease and is the single largest environmental health risk in Europe. Heart disease and stroke are the most common reasons for premature deaths attributable to air pollution, followed by lung diseases and lung cancer.
The health risk assessment methodology assumptions have been recently adapted to follow the recommendations by the World Health Organisation (WHO), released in 2021. The new global air quality guidelines by WHO provide up-to-date health-based guideline levels for major health-damaging air pollutants and new recommendations for assessing the risk of exposure to air pollution.
This report estimates the health risk related to air pollution in 2020 based on the latest methodology. The estimates consider the number of premature deaths and years of life lost related to exposure to fine particulate matter, ozone and nitrogen dioxide, both for the 27 Member States of the European Union and for additional 14 European countries (Albania, Andorra, Bosnia and Herzegovina, Iceland, Kosovo, Liechtenstein, Monaco, Montenegro, North Macedonia, Norway, San Marino, Serbia, Switzerland, and Türkiye).
A sensitivity analysis to the changes in concentration-response functions and counterfactual concentrations is performed to understand the impact of such changes on the mortality outcome estimates. The sensitivity analysis included both old and new health risk methodology assumptions but also the recommendation from the ELAPSE study on the concentration response functions. The ELAPSE project includes some of the most recent studies on the health effects at low air pollution levels by examining associations between exposures to relatively low levels of air pollution across Europe, including levels below the current EU standards.
The results for 2020 show that the largest health risks are estimated for the countries with the largest populations. However, in relative terms, when considering e.g., years of life lost per 100 000 inhabitants, the largest relative risks are observed in central and eastern European countries for PM2.5, in central and southern European countries for NO2, and south and eastern European for O3. The lowest impact is found for the northern and north-western parts of Europe, where the concentrations are lowest. The number of premature deaths attributed to air pollution in 2020 compared to 2019, increased for PM2.5 and decreased for NO2 and O3. Apart from the changes in concentrations and demographics, the COVID-19 pandemics seems to also have an influence on these changes. For PM2.5, the reduction in concentrations were counteracted by the excess of deaths due to the pandemics. In the case of NO2, the reduction in concentrations was more pronounced as a result of the lockdown measures and the drastic reduction in traffic and its impact in reducing mortality was bigger than the increasing impact of excess of deaths due to COVID-19.
Changing assumptions on concentration-response functions and counterfactual concentrations have implications for estimating mortality health outcomes. The sensitivity analysis shows that it is not straightforward to assess which assumptions estimates the highest health impacts when both factors change. In this case, the final outcome will depend on the concentration at the grid-cell level. The latest assumptions are expected to reduce the health outcomes for PM2.5 and increase for NO2 and O3, when compared to the previous one. When aggregated to all countries, the health outcomes are reduced by over 40 % for PM2.5 and increased by 50 % and 30 % for NO2 and O3, respectively, in 2020. However, this change varies across countries depending on the concentration level the population in the individual countries is exposed to.
ETC/HE
2022
Mercury in air and soil on an urban-rural transect in East Africa
There are large knowledge gaps concerning concentrations, sources, emissions, and spatial trends of mercury (Hg) in the atmosphere in developing regions of the Southern Hemisphere, particularly in urban areas. Filling these gaps is a prerequisite for assessing the effectiveness of international regulation and for enabling a better understanding of the global transport of Hg in the environment. Here we use a passive sampling technique to study the spatial distribution of gaseous elemental Hg (Hg(0), GEM) and assess emission sources in and around Dar es Salaam, Tanzania's largest city. Included in the study were the city's main municipal waste dumpsite and an e-waste processing facility as potential sources of GEM. To complement the GEM data and for a better overview of the Hg contamination status of Dar es Salaam, soil samples were collected from the same locations where passive air samplers were deployed and analysed for total Hg. Overall, GEM concentrations ranged between <0.86 and 5.34 ng m−3, indicating significant local sources within the urban area. The municipal waste dumpsite and e-waste site had GEM concentrations elevated above the background, at 2.41 and 1.77 ng m−3, respectively. Hg concentrations in soil in the region (range 0.0067 to 0.098 mg kg−1) were low compared to those of other urban areas and were not correlated with atmospheric GEM concentrations. This study demonstrates that GEM is a significant environmental issue in the urban region of Dar es Salaam. Further studies from urban areas in the Global South are needed to better identify sources of GEM.
2022